Rapid detection and differentiation method of VanA, VanB and VanC phenotypes in vancomycin-resistant enterococci

被引:7
|
作者
Hanaki, H [1 ]
Yamaguchi, Y
Nomura, S
Nagayama, A
Sunakawa, K
机构
[1] Kitasato Inst, Infect Control Lab, Tokyo 1080072, Japan
[2] Kitasato Univ, Sch Med, Dept Infect Dis, Kanagawa, Japan
[3] Nakamuragakuen Univ, Dept Nutr, Lab Clin Bacteriol, Jyonan Ku, Fukuoka, Japan
[4] Fukuoka Univ, Sch Med, Dept Microbiol, Fukuoka, Japan
关键词
vancomycin-resistant enterococci; teicoplanin; vancomycin; polymerase chain reaction;
D O I
10.1016/j.ijantimicag.2003.09.031
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
We developed a simple method that can replace the polymerase chain reaction (PCR) to distinguish between vancomycin-resistant enterococci (VRE) with the vanA, vanB and vanC genes. The method is based on induction of teicoplanin resistance by vancomycin in vanB-VRE, while the two compounds have a synergistic effect in vanC-VRE. In addition, vanA-VRE shows resistance to both vancomycin and teicoplanin, and both the compounds can induce resistance to vanA-VRE. Utilising these properties, we attempted to develop a simple method to distinguish between vanA, vanB and vanC. We compared our simple method with the PCR method in 43 strains of vanA-VRE, 35 strains of vanB-VRE and 37 strains of vanC-VRE. The results were 100% consistent with that obtained by PCR. (C) 2004 Elsevier B.V. and the International Society of Chemotherapy. All rights reserved.
引用
收藏
页码:502 / 505
页数:4
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